Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Dennis C. Argentieri"'
Autor:
Todd C. Henninger, Dennis J. Hlasta, Michael P. Wachter, Dennis C. Argentieri, Michele A. Weidner-Wells, Michele Matheis, David M. Ritchie, Christine M. Boggs, Stephanie A. Fraga-Spano
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:4307-4311
A novel series of 3,5-diarylisoxazole and 3,5-diaryl-1,2,4-oxadiazole IL-8 inhibitors has been identified. These compounds exhibit activity in an IL-8 binding assay as well as in a functional assay of IL-8 induced elastase release from neutrophils. I
Autor:
Jill M. Carton, Dennis C. Argentieri, Bruce P. Damiano, Michael R. D'Andrea, David J. Uhlinger
Publikováno v:
Thrombosis and Haemostasis. 86:1320-1326
SummaryThe response to vascular injury is a complex wound healing response involving cell proliferation, migration, remodeling and inflammation. In the present studies we employed a rat balloon angioplasty model of vascular injury to investigate the
Autor:
Wei Wu, Michael P. Wachter, Dennis C. Argentieri, Elizabeth A. Malloy, Arminda G. Barbone, Michele Steber, Justin Ansell, David M. Ritchie, Thomas Kirchner, Monica Singer, Scott A. Beers
Publikováno v:
Bioorganic & Medicinal Chemistry. 5:779-786
Compound 4k N-[5-(4-fluoro)phenoxythien-2-yl]methanesulfonamide is representative of a new class of potent inhibitors of 5-lipoxygenase (5-LO). These versatile compounds exhibit dose-dependent inhibition of 5-LO with IC50s ranging from 20–100 nM in
Autor:
Scott A. Waldman, Ian L. Smith, Thorir D. Bjornsson, John Misiti, Cheryl Vitow, Andrew T. Chow, Barbara Osborne, Francis A. Wong, Lisa Gillen, Dennis C. Argentieri
Publikováno v:
The Journal of Clinical Pharmacology. 36:462-468
This study was conducted to examine the pharmacokinetics and pharmacodynamics of tepoxalin in healthy volunteers, an antiinflammatory compound that inhibits cyclooxygenase and lipoxygenase. Tepoxalin was absorbed after oral administration of single d
Autor:
Charlene D. Connelly, Ian L. Smith, Monica Singer, Dennis C. Argentieri, Robert B. Raffa, James J. Schupsky, Rebecca P. Martinez
Publikováno v:
Drug Development Research. 36:81-90
Tepoxalin is a novel dual inhibitor of cyclooxygenase (CO) and lipoxygenase (LO) pathways of arachidonic acid metabolism with a relative lack of gastrointestinal side effects within its preclinical therapeutic dose range. The present study investigat
Autor:
Monica Singer, Michael Paul Ferro, Michele Steber, Dennis C. Argentieri, Michael P. Wachter, Kathy McCoy, William V. Murray, Dave M. Ritchie, Jihua Guan, Zhihua Sui
Publikováno v:
ChemInform. 31
Novel 1,3-diarylcycloalkanopyrazoles 1, and diphenyl hydrazides 2 were identified as selective inhibitors of cyclooxygenase-2. The 1,3-diaryl substitution pattern of the pyrazole ring in 1 differentiates these compounds from most of the known selecti
Autor:
Michael P. Wachter, Monica Singer, Dennis C. Argentieri, Eugene B. Grant, Deodialsingh Guiadeen, Dennis J. Hlasta
Publikováno v:
ChemInform. 33
The failure to fully regulate the inflammation response has been linked to diseases such as rheumatoid arthritis, septic shock syndrome, and asthma. The human complement system initiates and regulates the inflammation response through a cascade of re
Autor:
Xun Li, Bangping Xiang, Kristin M. Averill, Wai Ping Leung, Bohumila Fahmy, Paul F. Jackson, Dennis C. Argentieri, Hall Daniel A, John Siekierka, Xiaodong Fan, Thomas Razler, James L. Bullington, Gilbert C. Olini, Michael Reuman, Ping Ling, Demetrius Carter, Russell Wolff, Geoffrey R. Heintzelman, Druie Cavender, Scott A. Wadsworth, Kenneth C. Rupert, Ronald K. Russell, Yue Mei Zhang
Publikováno v:
Bioorganicmedicinal chemistry letters. 16(23)
Inhibition of the p38 map kinase pathway has been shown to be beneficial in the treatment of inflammatory diseases. The first class of potent p38 kinase inhibitors was the pyridinylimidazole compounds from SKB. Since then several pyridinylimidazole-b
Autor:
Rathna Thyagarajan, John Siekierka, Robert Falotico, Demetrius Carter, Dennis C. Argentieri, Tom Jay Parry, Ruth Brosius
Publikováno v:
European journal of pharmacology. 524(1-3)
Sirolimus and paclitaxel eluted from stents inhibit cell proliferation and other cellular processes by dramatically different mechanisms. In this study, the effects of sirolimus and paclitaxel on cultured human coronary artery smooth muscle and endot
Autor:
Robert Falotico, Rathna Thyagarajan, John Siekierka, Dennis C. Argentieri, Tom Jay Parry, Ronald J. Tallarida
Publikováno v:
European journal of pharmacology. 532(1-2)
Although sirolimus is a potent inhibitor of vascular smooth muscle cell (VSMC) proliferation and is effective at preventing restenosis in the majority of clinical revascularization procedures employing sirolimus-eluting stents, some VSMC may escape t